phf2[All Fields] AND 1[has_clinical] - dbVar

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Number of Variants: 20

Variant Region ID	Type	Number of Variant Calls	Study ID	Organism	Clinical Assertion	Location	Genes in region
nsv6291119	copy number variation	1	nstd102	human	Uncertain significance	GRCh37 chr9: 96,245,902-96,568,421 , GRCh38.p12 chr9: 93,483,620-93,806,139	PHF2, MIR548AU, 2 more genes
nsv3913446	copy number variation	1	nstd102	human	Uncertain significance	NCBI36 chr6: 33,491,109-33,508,684 , GRCh38 chr6: 33,415,354-33,432,929 , GRCh37 chr6: 33,383,131-33,400,706	CUTA, SYNGAP1, 1 more genes
nsv6315179	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 93,864,974-106,661,581 , GRCh38.p12 chr9: 91,102,692-103,899,300	PHF2, SUGT1P4-STRA6LP, 255 more genes
nsv4684256	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 96,126,075-108,535,272 , GRCh38.p12 chr9: 93,363,793-105,772,991	PHF2, RPS26P37, 238 more genes
nsv3922615	copy number variation	1	nstd102	human	Pathogenic	GRCh38 chr9: 91,596,533-97,018,746 , GRCh37 chr9: 94,358,815-99,781,028 , NCBI36 chr9: 93,398,636-98,820,849	PHF2, LOC107987097, 137 more genes
nsv6637944	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 95,711,603-98,469,214 , GRCh38.p12 chr9: 92,949,321-95,706,932	PHF2, MIRLET7D, 60 more genes
nsv3877040	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 60,107-171,054,786 , GRCh38.p12 chr6: 60,107-170,745,698	LOC105378061, MIR4640, 2914 more genes
nsv3879811	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 108,666-170,980,171 , GRCh38.p12 chr6: 108,666-170,671,083	RNU6-411P, LOC107986611, 2910 more genes
nsv3887898	copy number variation	2	nstd102	human	Pathogenic	GRCh37 chr6: 156,975-170,919,482 , GRCh38.p12 chr6: 156,975-170,610,394	SOD1P1, HLA-DPB1, 2905 more genes
nsv3889814	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr6: 165,632-170,919,470 , GRCh38.p12 chr6: 165,632-170,610,382	ITPR3, HSD17B8, 2905 more genes
nsv3912247	copy number variation	1	nstd102	human	Pathogenic	NCBI36 chr9: 2,934-140,273,252 , GRCh37.p13 chr9: 12,934-141,153,431 , GRCh38.p12 chr9: 12,934-138,262,981	PHF2, ALOX15P2, 2184 more genes
nsv3890420	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,122,247 , GRCh38.p12 chr9: 10,590-138,231,797	PHF2, TBC1D13, 2183 more genes
nsv3905118	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,114,095 , GRCh38.p12 chr9: 10,590-138,223,645	PHF2, MIR219A2, 2183 more genes
nsv3891842	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 10,590-141,107,672 , GRCh38.p12 chr9: 10,590-138,217,222	PHF2, OR13C1P, 2183 more genes
nsv3895453	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 46,587-141,066,491 , GRCh38.p12 chr9: 46,587-138,172,039	PHF2, RPL19P15, 2176 more genes
nsv3900967	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 163,131-141,122,114 , GRCh38.p12 chr9: 163,131-138,231,664	PHF2, BANCR, 2173 more genes
nsv3907479	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 62,525-141,006,407 , GRCh38.p12 chr9: 62,525-138,111,955	PHF2, OR2AM1P, 2174 more genes
nsv3922684	copy number variation	2	nstd102	human	Pathogenic	NCBI36 chr9: 194,193-140,193,718 , GRCh38 chr9: 193,412-138,179,445 , GRCh37 chr9: 204,193-141,073,897	PHF2, TDRD7, 2170 more genes
nsv3919257	copy number variation	1	nstd102	human	Pathogenic	GRCh37 chr9: 204,193-141,073,897 , GRCh38 chr9: 204,193-138,179,445 , NCBI36 chr9: 194,193-140,193,718	PHF2, LOC107987031, 2169 more genes
nsv3915973	copy number variation	2	nstd102	human	Pathogenic	GRCh38 chr9: 193,412-138,159,073 , GRCh37 chr9: 68,420,641-141,053,525 , NCBI36 chr9: 67,910,461-140,173,346	PHF2, CTNNAL1, 2170 more genes

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dbVar

Result Filters

Object Type

Organism

Variant Type

Method Type

Clinical Interpretation

Has Clinical Interpretation

Sex of Subject

Origin

Study Type

Subject Phenotype Status

Additional filters

Search results

Items: 1 to 20 of 52

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Number of Variants: 20

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